TWI526442B - 新的具有β２腎上腺素增效劑及Ｍ３毒蕈碱拮抗劑之活性的環己胺衍生物 - Google Patents

新的具有β２腎上腺素增效劑及Ｍ３毒蕈碱拮抗劑之活性的環己胺衍生物 Download PDF

Info

Publication number: TWI526442B
Authority: TW; Taiwan
Prior art keywords: amino; methyl; hydroxy; oxy; ethyl
Prior art date: 2010-05-13

Application number

TW100116155A

Other languages

English (en)

Chinese (zh)

Other versions

TW201139424A (en

Inventor

奎諾尼斯馬利亞普雷特

寶西爾維亞風格納

杜蘭卡羅斯普伊格

阿瑪多文賽斯勞路門洛斯

博世荷西艾瓜德

賈伐羅伊裘安法蘭西斯可卡圖拉

Original Assignee

艾美羅有限公司

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2010-05-13

Filing date

2011-05-09

Publication date

2016-03-21

2011-05-09 Application filed by 艾美羅有限公司 filed Critical 艾美羅有限公司

2011-11-16 Publication of TW201139424A publication Critical patent/TW201139424A/zh

2016-03-21 Application granted granted Critical

2016-03-21 Publication of TWI526442B publication Critical patent/TWI526442B/zh

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230000000694 effects Effects 0.000 title claims description 39
229940121948 Muscarinic receptor antagonist Drugs 0.000 title claims description 14
239000003149 muscarinic antagonist Substances 0.000 title claims description 13
239000000048 adrenergic agonist Substances 0.000 title 1
150000003946 cyclohexylamines Chemical class 0.000 title 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 428
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 329
-1 (di-2-thienyl) ruthenium acetate Chemical compound 0.000 claims description 256
150000001875 compounds Chemical class 0.000 claims description 247
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 200
125000000217 alkyl group Chemical group 0.000 claims description 110
239000000203 mixture Substances 0.000 claims description 105
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 64
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 62
239000003814 drug Substances 0.000 claims description 48
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 46
OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 39
GUTQMBQKTSGBPQ-UHFFFAOYSA-N dithiophen-2-ylmethanone Chemical group C=1C=CSC=1C(=O)C1=CC=CS1 GUTQMBQKTSGBPQ-UHFFFAOYSA-N 0.000 claims description 38
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 32
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 30
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 29
125000001424 substituent group Chemical group 0.000 claims description 23
238000011282 treatment Methods 0.000 claims description 21
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 19
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 18
201000010099 disease Diseases 0.000 claims description 17
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 17
125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims description 17
108010014499 beta-2 Adrenergic Receptors Proteins 0.000 claims description 16
125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 16
239000001257 hydrogen Substances 0.000 claims description 15
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229910052801 chlorine Inorganic materials 0.000 claims description 14
125000004093 cyano group Chemical group *C#N 0.000 claims description 14
125000001544 thienyl group Chemical group 0.000 claims description 14
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 12
125000001309 chloro group Chemical group Cl* 0.000 claims description 11
125000000031 ethylamino group Chemical group [H]C([H])([H])C([H])([H])N([H])[*] 0.000 claims description 11
125000004430 oxygen atom Chemical group O* 0.000 claims description 11
208000006545 Chronic Obstructive Pulmonary Disease Diseases 0.000 claims description 10
208000006673 asthma Diseases 0.000 claims description 10
125000004432 carbon atom Chemical group C* 0.000 claims description 10
125000003161 (C1-C6) alkylene group Chemical group 0.000 claims description 9
229940123932 Phosphodiesterase 4 inhibitor Drugs 0.000 claims description 9
DSAWYFXJVXQFIV-UHFFFAOYSA-N aminoazanium;fluoride Chemical compound [F-].[NH3+]N DSAWYFXJVXQFIV-UHFFFAOYSA-N 0.000 claims description 9
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208000019693 Lung disease Diseases 0.000 claims description 8
YFHNDHXQDJQEEE-UHFFFAOYSA-N acetic acid;hydrazine Chemical compound NN.CC(O)=O YFHNDHXQDJQEEE-UHFFFAOYSA-N 0.000 claims description 8
229910052757 nitrogen Inorganic materials 0.000 claims description 7
239000008194 pharmaceutical composition Substances 0.000 claims description 7
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 6
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 6
208000010412 Glaucoma Diseases 0.000 claims description 6
206010061218 Inflammation Diseases 0.000 claims description 6
208000012902 Nervous system disease Diseases 0.000 claims description 6
208000025966 Neurological disease Diseases 0.000 claims description 6
125000003545 alkoxy group Chemical group 0.000 claims description 6
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 6
239000003246 corticosteroid Substances 0.000 claims description 6
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 6
125000005843 halogen group Chemical group 0.000 claims description 6
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230000001575 pathological effect Effects 0.000 claims description 5
125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 claims description 4
229910052799 carbon Inorganic materials 0.000 claims description 4
229910052731 fluorine Inorganic materials 0.000 claims description 4
229910000040 hydrogen fluoride Inorganic materials 0.000 claims description 4
YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims description 3
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125000004429 atom Chemical group 0.000 claims description 3
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238000004519 manufacturing process Methods 0.000 claims description 3
125000004433 nitrogen atom Chemical group N* 0.000 claims description 3
229940049953 phenylacetate Drugs 0.000 claims description 3
WLJVXDMOQOGPHL-UHFFFAOYSA-N phenylacetic acid Chemical compound OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 claims description 3
YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Natural products C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 claims description 2
208000005107 Premature Birth Diseases 0.000 claims description 2
206010036590 Premature baby Diseases 0.000 claims description 2
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
239000003085 diluting agent Substances 0.000 claims description 2
125000001153 fluoro group Chemical group F* 0.000 claims description 2
UMSOZXHRARPZGE-UHFFFAOYSA-N hydrazine;dihydrofluoride Chemical compound F.F.NN UMSOZXHRARPZGE-UHFFFAOYSA-N 0.000 claims description 2
125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims description 2
125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 1
102100039705 Beta-2 adrenergic receptor Human genes 0.000 claims 1
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125000003277 amino group Chemical group 0.000 claims 1
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208000010643 digestive system disease Diseases 0.000 claims 1
208000018685 gastrointestinal system disease Diseases 0.000 claims 1
HYKHMHDNVZXOPH-UHFFFAOYSA-N ruthenium hydrofluoride Chemical compound [Ru].F HYKHMHDNVZXOPH-UHFFFAOYSA-N 0.000 claims 1
239000003451 thiazide diuretic agent Substances 0.000 claims 1
239000000543 intermediate Substances 0.000 description 475
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 250
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 142
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 126
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238000002474 experimental method Methods 0.000 description 52
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239000002904 solvent Substances 0.000 description 49
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238000002360 preparation method Methods 0.000 description 43
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238000005481 NMR spectroscopy Methods 0.000 description 35
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AQHHHDLHHXJYJD-UHFFFAOYSA-N propranolol Chemical compound C1=CC=C2C(OCC(O)CNC(C)C)=CC=CC2=C1 AQHHHDLHHXJYJD-UHFFFAOYSA-N 0.000 description 11
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238000010998 test method Methods 0.000 description 1
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FPGGTKZVZWFYPV-UHFFFAOYSA-M tetrabutylammonium fluoride Chemical compound [F-].CCCC[N+](CCCC)(CCCC)CCCC FPGGTKZVZWFYPV-UHFFFAOYSA-M 0.000 description 1
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238000005809 transesterification reaction Methods 0.000 description 1
229960005294 triamcinolone Drugs 0.000 description 1
GFNANZIMVAIWHM-OBYCQNJPSA-N triamcinolone Chemical compound O=C1C=C[C@]2(C)[C@@]3(F)[C@@H](O)C[C@](C)([C@@]([C@H](O)C4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 GFNANZIMVAIWHM-OBYCQNJPSA-N 0.000 description 1
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YNDXUCZADRHECN-JNQJZLCISA-N triamcinolone acetonide Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@]2(F)[C@@H]1[C@@H]1C[C@H]3OC(C)(C)O[C@@]3(C(=O)CO)[C@@]1(C)C[C@@H]2O YNDXUCZADRHECN-JNQJZLCISA-N 0.000 description 1
CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 1
229940029284 trichlorofluoromethane Drugs 0.000 description 1
UCPYLLCMEDAXFR-UHFFFAOYSA-N triphosgene Chemical compound ClC(Cl)(Cl)OC(=O)OC(Cl)(Cl)Cl UCPYLLCMEDAXFR-UHFFFAOYSA-N 0.000 description 1
YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
NSBGJRFJIJFMGW-UHFFFAOYSA-N trisodium;stiborate Chemical compound [Na+].[Na+].[Na+].[O-][Sb]([O-])([O-])=O NSBGJRFJIJFMGW-UHFFFAOYSA-N 0.000 description 1
125000002221 trityl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C([*])(C1=C(C(=C(C(=C1[H])[H])[H])[H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
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238000004704 ultra performance liquid chromatography Methods 0.000 description 1
210000001635 urinary tract Anatomy 0.000 description 1
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210000001186 vagus nerve Anatomy 0.000 description 1
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239000000052 vinegar Substances 0.000 description 1
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239000002023 wood Substances 0.000 description 1
BPICBUSOMSTKRF-UHFFFAOYSA-N xylazine Chemical compound CC1=CC=CC(C)=C1NC1=NCCCS1 BPICBUSOMSTKRF-UHFFFAOYSA-N 0.000 description 1
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229910052725 zinc Inorganic materials 0.000 description 1
239000011701 zinc Substances 0.000 description 1
GTLDTDOJJJZVBW-UHFFFAOYSA-N zinc cyanide Chemical compound [Zn+2].N#[C-].N#[C-] GTLDTDOJJJZVBW-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
- A—HUMAN NECESSITIES
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
- A—HUMAN NECESSITIES
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/472—Non-condensed isoquinolines, e.g. papaverine
- A61K31/4725—Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P1/06—Anti-spasmodics, e.g. drugs for colics, esophagic dyskinesia
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P11/06—Antiasthmatics
- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P11/08—Bronchodilators
- A—HUMAN NECESSITIES
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- A61P15/06—Antiabortive agents; Labour repressants
- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/20—Oxygen atoms
- C07D215/24—Oxygen atoms attached in position 8
- C07D215/26—Alcohols; Ethers thereof
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Veterinary Medicine (AREA)
Public Health (AREA)
General Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Animal Behavior & Ethology (AREA)
Pharmacology & Pharmacy (AREA)
General Chemical & Material Sciences (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Chemical Kinetics & Catalysis (AREA)
Bioinformatics & Cheminformatics (AREA)
Engineering & Computer Science (AREA)
Pulmonology (AREA)
Epidemiology (AREA)
Neurosurgery (AREA)
Ophthalmology & Optometry (AREA)
Pain & Pain Management (AREA)
Biomedical Technology (AREA)
Neurology (AREA)
Heart & Thoracic Surgery (AREA)
Gynecology & Obstetrics (AREA)
Pregnancy & Childbirth (AREA)
Endocrinology (AREA)
Reproductive Health (AREA)
Rheumatology (AREA)
Cardiology (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Plural Heterocyclic Compounds (AREA)
Quinoline Compounds (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Hydrogenated Pyridines (AREA)
Medicines Containing Plant Substances (AREA)

TW100116155A 2010-05-13 2011-05-09 新的具有β２腎上腺素增效劑及Ｍ３毒蕈碱拮抗劑之活性的環己胺衍生物 TWI526442B (zh)

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EP10382118A EP2386555A1 (fr)	2010-05-13	2010-05-13	Nouveaux dérivés de cyclohéxylamine dotés d'activités agoniste bêta 2 adrénergique et antagoniste muscarinique m3

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TW201139424A TW201139424A (en)	2011-11-16
TWI526442B true TWI526442B (zh)	2016-03-21

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Country Status (38)

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US (1)	US9643961B2 (fr)
EP (2)	EP2386555A1 (fr)
JP (1)	JP5851489B2 (fr)
KR (1)	KR101756497B1 (fr)
CN (1)	CN102892765B (fr)
AR (1)	AR081387A1 (fr)
AU (1)	AU2011252337C1 (fr)
BR (1)	BR112012026570A2 (fr)
CA (1)	CA2799099C (fr)
CL (1)	CL2012003171A1 (fr)
CO (1)	CO6592031A2 (fr)
CR (1)	CR20120574A (fr)
CY (1)	CY1118352T1 (fr)
DK (1)	DK2569308T3 (fr)
EA (1)	EA022358B1 (fr)
EC (1)	ECSP12012213A (fr)
ES (1)	ES2613355T3 (fr)
GT (1)	GT201200307A (fr)
HR (1)	HRP20170307T1 (fr)
HU (1)	HUE033244T2 (fr)
IL (1)	IL222538A (fr)
LT (1)	LT2569308T (fr)
ME (1)	ME02675B (fr)
MX (1)	MX2012012897A (fr)
MY (1)	MY171899A (fr)
NZ (1)	NZ602556A (fr)
PE (1)	PE20130215A1 (fr)
PH (1)	PH12012502237A1 (fr)
PL (1)	PL2569308T3 (fr)
PT (1)	PT2569308T (fr)
RS (1)	RS55725B1 (fr)
SG (1)	SG185007A1 (fr)
SI (1)	SI2569308T1 (fr)
SM (2)	SMT201700022T1 (fr)
TW (1)	TWI526442B (fr)
UY (1)	UY33362A (fr)
WO (1)	WO2011141180A1 (fr)
ZA (1)	ZA201207031B (fr)

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Publication number	Publication date
PT2569308T (pt)	2017-02-24
ES2613355T3 (es)	2017-05-24
DK2569308T3 (da)	2017-02-20
ME02675B (fr)	2017-06-20
AR081387A1 (es)	2012-08-29
EP2569308A1 (fr)	2013-03-20
WO2011141180A8 (fr)	2012-01-19
JP5851489B2 (ja)	2016-02-03
EP2386555A1 (fr)	2011-11-16
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MY171899A (en)	2019-11-06
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IL222538A (en)	2015-11-30
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2023-12-21	MM4A	Annulment or lapse of patent due to non-payment of fees

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US20140303127A1 (en)	2014-10-09	New cyclohexylamine derivatives having beta 2 adrenergic agonist and m3 muscarinic antagonist activities
KR20150096732A (ko)	2015-08-25	베타2 아드레날린 아고니스트 및 ｍ3 무스카린 안타고니스트 활성을 갖는 새로운 시클로헥실 및 퀴누클리디닐 카르바메이트 유도체
JP2011517316A (ja)	2011-06-02	β２−アドレナリン受容体アゴニストとしての４−（２−アミノ−１−ヒドロキシエチル）フェノールの誘導体
WO2018108089A1 (fr)	2018-06-21	Classe de composés bifonctionnels de structure de sel d'ammonium quaternaire
HK1176929A (en)	2013-08-09	New cyclohexylamine derivatives having beta2 adrenergic agonist and m3 muscarinic antagonist activities
HK1176929B (en)	2017-09-29	New cyclohexylamine derivatives having beta2 adrenergic agonist and m3 muscarinic antagonist activities
HK1197241B (en)	2017-06-09	New cyclohexylamine derivatives having beta2 adrenergic agonist and m3 muscarinic antagonist activities
NZ624784B2 (en)	2015-09-29	New cyclohexylamine derivatives having ?2 adrenergic agonist and m3 muscarinic antagonist activities

TWI526442B - 新的具有β２腎上腺素增效劑及Ｍ３毒蕈碱拮抗劑之活性的環己胺衍生物 - Google Patents

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